Week 2: DNA Read, Write, and Edit

Week 2 cover Week 2 cover

Context
This page captures my Week 2 assignment for HTGAA 2025, reformatted for Hugo. Yellow callouts mark assignment prompts; red callouts (if any) would mark AI-assisted notes.


SynBio Read/Write/Edit — Homework

Warning

About your documentation
Document every step of your in-silico and lab work. Include sketches, screenshots, notes, and even failures (plus how you fixed them).

Part 0 — Basics of Gel Electrophoresis

Part 1 — Benchling & In-silico Gel Art

Follow the protocol and create an in-silico gel using a reference DNA (lambda).

Protocol & tools

Steps

  1. Get the lambda sequence / file

    • Use one of the references above to obtain the sequence (e.g., the SnapGene page).
    • Example (searching for lambda sequence):
      Search results for lambda dna sequence Search results for lambda dna sequence
    • Example (downloading a sequence/plasmid file):
      Download lambda.dna Download lambda.dna
  2. Add lambda DNA to Benchling

    • Import the FASTA/GenBank/SnapGene file into a new Benchling project (or paste the sequence).
    • Confirm length and cohesive ends are recognized (if provided by the source).
  3. Plan restriction digests

    • Choose enzymes that generate a distinctive band pattern for your gel “art”.
    • Record enzyme names, buffers, incubation plan, and expected fragment sizes.
  4. Simulate and export

    • Simulate the digest and generate expected band sizes.
    • Save screenshots of your enzyme map and gel preview.
  5. Design your gel art

    • Arrange lanes to create a pattern or message.
    • Add a ladder lane and any controls you need.
Tip

Deliverables for Part 1

  • Short write-up of your design idea.
  • Enzyme list + expected fragment sizes.
  • Screenshots: annotated sequence map and gel preview.
  • Notes on what worked/didn’t (troubleshooting).

Submission checklist

  • Overview paragraph explaining the intent of the gel art.
  • Sources cited for the lambda sequence.
  • Benchling screenshots (sequence map with restriction sites, gel preview).
  • Parameters: enzymes, buffer, temperature, time, and expected band sizes.
  • Reflection: mistakes, fixes, and next steps.